Microtumor models, combining cancer and stromal cells within 3D hydrogels, are vital for testing anticancer therapies. Bioprinting hydrogel scaffolds allows tailored in vitro models. We created a 3D microtumor model using a bioprinter, with varying ratios of ovarian stromal cells and leukemia cells (HL-60). PEGylated fibrinogen and alginate hydrogel were used. Cell dynamics and proliferation were assessed via immunofluorescence staining. Microtumors with different HL-60 ratios (1:1, 1:10, 1:100) were cultured for 5 days. Results showed tumor development modulation by cell ratios and culture time. A significant cell density increase occurred in 1:1 ratio microtumors, indicating rapid cancer cell proliferation. No HL-60 cells were found in 1:100 ratio microtumors by day 5. The 1:10 ratio closely mimicked leukemia invasion in ovarian tissue, showing detectable cancer cells by days 3 and 5 without altering total cell density dynamics significantly. This bioprinted leukemia microtumor model offers better physiological relevance than 2D assays, promising applications in cellular analysis and drug screening.
Keyphrases
- single cell
- cell therapy
- cell proliferation
- drug delivery
- acute myeloid leukemia
- induced apoptosis
- bone marrow
- stem cells
- signaling pathway
- endothelial cells
- emergency department
- tissue engineering
- oxidative stress
- cell cycle arrest
- papillary thyroid
- heavy metals
- cell migration
- young adults
- endoplasmic reticulum stress
- lymph node metastasis
- extracellular matrix
- drug release